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Prevention of diabetes in NOD mice treated with antibody to murine IFNγ

1991; Elsevier BV; Volume: 4; Issue: 2 Linguagem: Inglês

10.1016/0896-8411(91)90021-4

1095-9157

M Debray-Sachs, Claude Carnaud, Christian Boîtard, Hélène Cohen, Ion Gresser, Pierre Bédossa, Jean‐François Bach,

Diabetes Management and Research

The NOD mouse is studied as an animal model of human insulin-dependent diabetes mellitus (IDDM). To evaluate the role of IFNγ in the pathogenesis of the disease, we have studied the effect of anti-IFNγ mAb on the expression of insulitis and clinical diabetes. Treatment of mice with manti-IFNγ mAb prevented the induction of early IDDM by cyclophosphamide as well as the adoptive transfer of diabetes by spleen cells from diabetic NOD mice. The protection against induction of diabetes by cyclophosphamide was observed in animals treated with the anti-IFNγ mAb within 24 h following the first cyclophosphamide injection but not in animals in which mAb treatment was started 7 days later. Transfer of disease was prevented both in adult irradiated and in newborn recipients. The absence of clinical signs in these mice was corroborated by a significant reduction of both the extent and severity of insulitis. Over-expression of Ia antigen on endothelial cells lining the islets was also considerably reduced in mice treated with mAb. These data strongly suggest a role for IFNγ during the autoimmune process leading to β cell destruction in diabetes and prompt further investigation of the use of such antibodies in the immunoprevention of IDDM.